Archemin is a service provider to the pharma industry and helps the domestic and international Pharmaceutical Companies, Biotech Companies, Medical Device Manufacturers and Developers of Diagnostic Test Kits to bring their products to the market and keep them there.

We focus on the complex regulatory compliance requirements of our customers; provide regulatory affairs compliance, market access, validation and pharmacovigilance consulting and various other outsourced services to life sciences companies throughout the life cycle of their products.

In order to do so, our multidisciplinary specialist team:

• provides Drug Regulatory Affairs, Market Access, Pharmacovigilance and Clinical Research Services
• has access to a very extensive scientific library and several databases;
• has access to an effective pan-European network within the Pharmaceutical Industry, with Distributors, Contract Manufacturers, Certified Laboratories, CRO's and Service Providers;
• maintains excellent contacts with the Competent Authorities and University Experts;
• collaborates with an Expert Strategy and Evaluation Group whose members have many years of industry experience within the European Regulatory and Clinical Research Area.

Archemin is  member of  the International regulanet® Network.

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